Results 141 to 150 of about 68,902 (325)

Low-grade dorsal spinal cord astrocytoma presented with paraplegia following minor trauma

open access: yesSaudi Journal of Medicine and Medical Sciences, 2014
Although they constitute about one third of spinal cord glial neoplasms, low-grade astrocytomas can present variably. Post-traumatic neurologic dysfunction due to low-grade spinal cord gliomas is an uncommon event. The authors report a case of paraplegia
Bander F Al-Dhafery   +2 more
doaj   +1 more source

The hereditary spastic paraplegia-related enzyme DDHD2 is a principal brain triglyceride lipase

open access: yesProceedings of the National Academy of Sciences of the United States of America, 2014
Significance Many rare human genetic disorders are caused by mutations in genes that code for proteins of poorly characterized function. Determining the functions of these proteins is critical for understanding and devising potential treatments for human
Jordon M Inloes   +7 more
semanticscholar   +1 more source

Expanding the Phenotypic Spectrum of SPG7 Rare Damaging Variants: Insights From a Hungarian Cohort

open access: yesClinical Genetics, EarlyView.
Rare damaging SPG7 variants were detected in 58 patients with spastic paraplegia, ataxia, mitochondrial dysfunction, or motoneuron lesions. The cumulative prevalence of SPG7‐related conditions in Hungary was estimated. Phenotypic spectra and mitochondrial dysfunction were assessed in monoallelic and biallelic cases, contributing to the understanding of
Idris Janos Jimoh   +10 more
wiley   +1 more source

Enteric Paraplegia [PDF]

open access: yesThe Boston Medical and Surgical Journal, 1883
n ...
openaire   +2 more sources

Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia

open access: yesHuman Molecular Genetics, 2014
Hereditary spastic paraplegias are a group of inherited motor neuron diseases characterized by progressive paraparesis and spasticity. Mutations in the spastic paraplegia gene SPG11, encoding spatacsin, cause an autosomal-recessive disease trait; however,
Francesc Pérez-Brangulı́   +15 more
semanticscholar   +1 more source

Contributions of a University Extension Programme in Special Care Dentistry to Education and Training of Undergraduate Students: A Qualitative Study

open access: yesEuropean Journal of Dental Education, EarlyView.
ABSTRACT Background People with disabilities (PWD) have poor oral health and difficulties in accessing dental care. The lack of skills, willingness, or confidence of dentists to treat PWD could contribute to this scenario. Objective To understand the contributions of the Special Care Dentistry university extension programme to the professional and ...
Riéli Elis Schulz   +5 more
wiley   +1 more source

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